These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 36930806)

  • 1. Haemophilia B, severe childhood obesity and other extra-haematological features associated with similar 4Mb-deletions on Xq27: Clinical findings, molecular insights and literature update.
    Radic CP; Abelleyro MM; Ziegler B; Marchione VD; Nevado J; Lapunzina P; Sciuccati G; Neme D; Rossetti LC; Bonduel M; De Brasi CD
    Haemophilia; 2023 May; 29(3):844-854. PubMed ID: 36930806
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.
    Jourdy Y; Chatron N; Carage ML; Fretigny M; Meunier S; Zawadzki C; Gay V; Negrier C; Sanlaville D; Vinciguerra C
    J Thromb Haemost; 2016 Oct; 14(10):1988-1993. PubMed ID: 27477789
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.
    Radic CP; Rossetti LC; Abelleyro MM; Candela M; Pérez Bianco R; de Tezanos Pinto M; Larripa IB; Goodeve A; De Brasi C
    Thromb Haemost; 2013 Jan; 109(1):24-33. PubMed ID: 23093250
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterisation of large F9 deletions in seven unrelated patients with severe haemophilia B.
    Wu X; Lu Y; Ding Q; You G; Dai J; Xi X; Wang H; Wang X
    Thromb Haemost; 2014 Sep; 112(3):459-65. PubMed ID: 24816826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distinct X chromosomal rearrangements in four haemophilia B patients with entire F9 deletion.
    Nakamura Y; Ando Y; Takagi Y; Murata M; Kozuka T; Nakata Y; Hasebe R; Takagi A; Matsushita T; Shima M; Kojima T
    Haemophilia; 2016 May; 22(3):433-9. PubMed ID: 26686734
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The characteristics and spectrum of F9 mutations in Chinese sporadic haemophilia B pedigrees.
    Lu Y; Wu X; Dai J; Ding Q; Wu W; Wang X
    Haemophilia; 2019 Mar; 25(2):316-323. PubMed ID: 30648777
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B.
    Kwon MJ; Yoo KY; Kim HJ; Kim SH
    Haemophilia; 2008 Sep; 14(5):1069-75. PubMed ID: 18624698
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A genetic analysis of 23 Chinese patients with hemophilia B.
    Wang QY; Hu B; Liu H; Tang L; Zeng W; Wu YY; Cheng ZP; Hu Y
    Sci Rep; 2016 Apr; 6():25024. PubMed ID: 27109384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of two large duplications of F9 associated with mild and severe haemophilia B, respectively.
    Xie X; Chen C; Liang Q; Wu X; Wang X; Wu W; Ding Q
    Haemophilia; 2019 May; 25(3):475-483. PubMed ID: 30866119
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations.
    Huang L; Li L; Lin S; Chen J; Li K; Fan D; Jin W; Li Y; Yang X; Xiong Y; Li F; Yang X; Li M; Li Q
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1482. PubMed ID: 32875744
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations.
    Guo ZP; Yang LH; Qin XY; Liu XE; Chen JF; Zhang YF
    Haemophilia; 2014 Nov; 20(6):859-65. PubMed ID: 25251685
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complete F9 Gene Deletion, Duplication, and Triplication Rearrangements: Implications for Factor IX Expression and Clinical Phenotypes.
    Ma Y; Li Y; Sun J; Liang Q; Wu R; Ding Q; Dai J
    Thromb Haemost; 2024 Apr; 124(4):374-385. PubMed ID: 38011862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutations.
    Yu T; Dai J; Liu H; Ding Q; Lu Y; Wang H; Wang X; Fu Q
    Pathology; 2012 Jun; 44(4):342-7. PubMed ID: 22544209
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SOX3 deletion in mouse and human is associated with persistence of the craniopharyngeal canal.
    Alatzoglou KS; Azriyanti A; Rogers N; Ryan F; Curry N; Noakes C; Bignell P; Hall GW; Littooij AS; Saunders D; Thomas P; Stewart H; Dattani MT
    J Clin Endocrinol Metab; 2014 Dec; 99(12):E2702-8. PubMed ID: 25140394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B.
    Saini S; Hamasaki-Katagiri N; Pandey GS; Yanover C; Guelcher C; Simhadri VL; Dandekar S; Guerrera MF; Kimchi-Sarfaty C; Sauna ZE
    Haemophilia; 2015 Mar; 21(2):210-218. PubMed ID: 25470321
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes.
    Bastida JM; González-Porras JR; Jiménez C; Benito R; Ordoñez GR; Álvarez-Román MT; Fontecha ME; Janusz K; Castillo D; Fisac RM; García-Frade LJ; Aguilar C; Martínez MP; Bermejo N; Herrero S; Balanzategui A; Martin-Antorán JM; Ramos R; Cebeiro MJ; Pardal E; Aguilera C; Pérez-Gutierrez B; Prieto M; Riesco S; Mendoza MC; Benito A; Hortal Benito-Sendin A; Jiménez-Yuste V; Hernández-Rivas JM; García-Sanz R; González-Díaz M; Sarasquete ME
    Thromb Haemost; 2017 Jan; 117(1):66-74. PubMed ID: 27734074
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation Spectrum and Genotype-Phenotype Analyses in a Pakistani Cohort With Hemophilia B.
    Khan MTM; Naz A; Ahmed J; Shamsi T; Ahmed S; Ahmed N; Imran A; Farooq N; Khan MTH; Taj AS
    Clin Appl Thromb Hemost; 2018 Jul; 24(5):741-748. PubMed ID: 28752769
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mild haemophilia B from a novel missense mutation Ser350Ala of the F9 gene.
    Park CH; Seo JY; Kim SH; Koo HH; Kim HJ
    Blood Coagul Fibrinolysis; 2013 Jul; 24(5):544-6. PubMed ID: 23492913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohorts.
    Lassalle F; Marmontel O; Zawadzki C; Fretigny M; Bouvagnet P; Vinciguerra C
    Haemophilia; 2018 Jul; 24(4):e213-e221. PubMed ID: 29656491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effect.
    Jenkins PV; Egan H; Keenan C; O'Shea E; Smith OP; Nolan B; White B; O'Donnell J
    Haemophilia; 2008 Jul; 14(4):717-22. PubMed ID: 18479429
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.